After assigning the priority of each substitution, naming is done on alphabetical order with respect to the parental ring.
So parantal ring will be cyclohexane combined with most prior group- cyclohexanol.
ОН. Provide a name for the molecule shown. A 3-iodo-5-isopropoxyphenol B meta-iodo meta-isopropoxyphenol С 1-isopropoxy-3-hydroxy-5-iodocyclohexane D...
Select the correct lUPAC name for the following cycloalkane: 1, 3-diethyl-2-iodocyclohexane 2-iodo-1, 3-dipropylcyclohexane 1-iodo-2, 6-dipropylcyclohexane 2, 6-diethy-1-iodocyclohexane
What is the IUPAC name of this structure? OH A. (E)-6-hydroxy-3-methyloct-3-ene B. (E)-6-methyl-oct-5-en-3-ol C. (Z)-6-methyloct-5-en-3-ol D. (Z)-3-hydroxy-6-methyloct-5-ene Which is the major product of this reaction? NaOB Br OH wi он Br A B C D А B С OD
1. Draw the following molecules, based on their IUPAC name: a) 2-hydroxy-5, 5-dimethylheptanedioic acid; b) 3-hydroxy-7-methylnonanedioic acid 2. Give the IUPAC name for the following compounds: A) HO OH 3. Circle the name that is correct for each molecule, based on IUPAC rules. V a) 4-methylheptanoate 4-methylbutanoate b) pentyl 4-metylhexanoate c) 3-methylbutyl 4-methylhexanoate d) isobutyl 4-methylhexanoate
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral (meso) compounds below. (4 points) OH COH HOZC OH c. Draw the structure of the compound based on its IUPAC name. (4 points) d. Of the cations below, circle any that are achiral. (4 points) OAC Hg ΤΗ (E)-4-ethyl-3-fluorohept-3-ene e. Provide the IUPAC name of the molecule shown below. (4 points) f Rank the following cations from least stable to most stable. (3 points)...
Question 5 1 pts ҫнон но с н The molecule to the right is a(n) Н—с—он н—с—он сH,он Pyrane Aldose Furane Ketose
5. How many chirality centers (stereocenters) are in this molecule? Ноо он но он А) 1 В. 2 С. 3 D. 4 E. 5
1. (12 points) Provide the IUPAC name for each molecule shown: нсон CHE CH3 CH₂ d. (CH).CCH=CCl2 Hz нус 2. (12 points) Provide a structure for each named molecule: a. cis-3-bromocylopentanol C. 2-cyclobutyl-2-propanol b. (E)-3-chloro-3-heptene d. trans-1,2-divinylcyclohexane 1 Pa
1. PROVIDE REAGENTS NEEDED FOR THE FOLLOWING TRANSFORMATIONS: ОН ОН ОН Ph но - НО,С LUNG MOLECULE USING ANY STARTING ALCOHOL FEWER THAN GENTS. (YOU CAN USE ANY SOLVENT) SENTNESS OF INE FOLLOWING MOLECULES PRE 3. PROVIDE FINAL PRODUCTS 1. Br, hy 2. C2H2, NaNH2 3. BH3-THF then H2O2, NaOH 4. Vinyllithium, Et, 5. H3PO4, A 1. Licu 2. HBr 2. 3. Mgº, Ether 4. CO2, then H307 1. PROVIDE REAGENTS NEEDED FOR DE REAGENTS NEEDED FOR THE FOLLOWING TRANSFORMATIONS:...
1) Provide the two best resonance structures of the molecule shown below. a) оснз b) он
Name the following compounds
Acids and Esters homework. 1. Name the following Compounds он OH Brown golon он MacBook A 0. % 5 A 6 7 B 9 0 3 2 P W E R U T Y S D А F G Н. K ? Z с - V N B M Command option option command он OH НО- OH o D MacBook Air A * $ 4 % 5 & 7 3 6 8 9 0 W E...